Colon Cancer: Gene >> CNDP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358821
Start	74576886:74576886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.859T>C
AA Mutation	p.Ser287Pro(p.S287P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358821
Start	74559349:74559349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.180G>T
AA Mutation	p.Glu60Asp(p.E60D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358821
Start	74578274:74578274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1114A>C
AA Mutation	p.Lys372Gln(p.K372Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358821
Start	74567387:74567387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.710C>G
AA Mutation	p.Pro237Arg(p.P237R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358821
Start	74556408:74556408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762793335
CDS Mutation	c.95C>T
AA Mutation	p.Pro32Leu(p.P32L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358821
Start	74556354:74556354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200702092
CDS Mutation	c.41C>T
AA Mutation	p.Ala14Val(p.A14V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358821
Start	74577020:74577020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532473359
CDS Mutation	c.993C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358821
Start	74556412:74556412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780586369
CDS Mutation	c.99G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358821
Start	74559433:74559433(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.268delG
AA Mutation	p.Ala90ProfsTer62(p.A90Pfs*62)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358821
Start	74567340:74567341(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.664_665insTTTG
AA Mutation	p.Asp222ValfsTer2(p.D222Vfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CNDP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358821
Start	74567324:74567324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200332997
CDS Mutation	c.647G>A
AA Mutation	p.Arg216Gln(p.R216Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358821
Start	74577021:74577021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148917348
CDS Mutation	c.994G>A
AA Mutation	p.Asp332Asn(p.D332N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358821
Start	74577020:74577020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532473359
CDS Mutation	c.993C>T
Mutation Classification	Silent
Feature Type	Transcript